About   Help   FAQ
Grin2ctm2Rsp
Targeted Allele Detail
Summary
Symbol: Grin2ctm2Rsp
Name: glutamate receptor, ionotropic, NMDA2C (epsilon 3); targeted mutation 2, Rolf Sprengel
MGI ID: MGI:3850683
Synonyms: NR2C-
Gene: Grin2c  Location: Chr11:115139995-115158069 bp, - strand  Genetic Position: Chr11, 80.8 cM
Alliance: Grin2ctm2Rsp page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:45446
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
    A neomycin selection cassette replaced a part of intron 4 and exon 5. (J:45446)
Inheritance:    Recessive
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Grin2c Mutation:  56 strains or lines available
References
Original:  J:45446 Sprengel R, et al., Importance of the intracellular domain of NR2 subunits for NMDA receptor function in vivo. Cell. 1998 Jan 23;92(2):279-89
All:  3 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
12/10/2024
MGI 6.24
The Jackson Laboratory